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O-Cal-ette
PHARMICS, INC. · Model 9900 · UDI-DI 00308130099001
10
510(k) clearances
18
Adverse events
1
Recalls
51
Facilities
Description
Nursing Cup
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-05-18 | Medela Inc | The product sterility may be compromised due to possible pinholes in the rigid tray of the package. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.